RGD:8587080 Rat Genome Database

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Variant: RGD:8587080 -  Homo sapiens

RGD ID: 8587080
ClinVar ID: CV121706
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGAP6  LOC124905246  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 11,435,766
GRCh38 X 11,417,646
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_013427.2:c.589-162939A>T
NG_012494.1:g.253056A>T
NC_000023.11:g.11417646T>A
NC_000023.10:g.11435766T>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:LOC124905246
Accession:XR_007068392
Location:EXON;NON-CODING

Gene Symbol:ARHGAP6
Accession:NM_013427
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NM_006125
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NM_001287242
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NM_013423
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NR_109776
Location:INTRON;NON-CODING

Variant Samples